ネチルマイシン硫酸塩

ネチルマイシン硫酸塩 化学構造式
56391-57-2
CAS番号.
56391-57-2
化学名:
ネチルマイシン硫酸塩
别名:
ネトロマイシン硫酸塩;硫酸ネチルマイシン;4-O-[[3α-アミノ-6-(アミノメチル)-3,4-ジヒドロ-2H-ピラン]-2α-イル]-6-O-[4-C-メチル-3-(メチルアミノ)-3-デオキシ-β-L-アラビノピラノシル]-N1-エチル-2-デオキシ-D-ストレプタミン·2.5硫酸塩;ネチルミシン硫酸塩;ネチルマイシン硫酸塩;硫酸ネチルミシン;ネチルマイシン 硫酸塩;ネチルマイシン硫酸塩 (JAN)
英語名:
Netilmicin sulfate
英語别名:
netromycin;Netromicine;NETILMYCIN SULFATE;Netililn;Zetamicin;Sulfate NetilMicin;sulfate(2:5)(salt);Netromycin sulfate;1-N-ETHYLSISOMICIN;NETILMICIN SULFATE
CBNumber:
CB7121612
化学式:
C42H92N10O34S5
分子量:
1441.55
MOL File:
56391-57-2.mol
MSDS File:
SDS

ネチルマイシン硫酸塩 物理性質

融点 :
>194°C (dec.)
沸点 :
868℃
貯蔵温度 :
Inert atmosphere,2-8°C
溶解性:
H2O: 可溶性10mg/mL
外見 :
個体
色:
白色~微黄色
水溶解度 :
水に溶ける
Sensitive :
Light Sensitive & Hygroscopic
安定性::
吸湿性
EPAの化学物質情報:
Netilmicin sulfate (56391-57-2)
安全性情報
  • リスクと安全性に関する声明
  • 危険有害性情報のコード(GHS)
主な危険性  T,Xi
Rフレーズ  61-20/21/22-60
Sフレーズ  53-36/37/39-45-37/39-36-26
WGK Germany  3
RTECS 番号 WK2286000
HSコード  2941906000
絵表示(GHS) GHS hazard pictograms
注意喚起語 危険
危険有害性情報
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード
H360 生殖能または胎児への悪影響のおそれ 生殖毒性 1A, 1B 危険 GHS hazard pictograms
注意書き
P201 使用前に取扱説明書を入手すること。
P202 全ての安全注意を読み理解するまで取り扱わないこ と。
P280 保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。
P308+P313 暴露または暴露の懸念がある場合:医師の診断/手当てを 受けること。
P405 施錠して保管すること。
P501 内容物/容器を...に廃棄すること。

ネチルマイシン硫酸塩 価格 もっと(12)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01LKTN1976 硫酸ネチルマイシン
Netilmicin Sulfate
56391-57-2 5mg ¥67100 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01LKTN1976 硫酸ネチルマイシン
Netilmicin Sulfate
56391-57-2 10mg ¥100600 2024-03-01 購入
東京化成工業 N1108 ネチルマイシン硫酸塩 >98.0%(HPLC)
Netilmicin Sulfate >98.0%(HPLC)
56391-57-2 25mg ¥13900 2024-03-01 購入
東京化成工業 N1108 ネチルマイシン硫酸塩 >98.0%(HPLC)
Netilmicin Sulfate >98.0%(HPLC)
56391-57-2 100mg ¥40200 2024-03-01 購入
Sigma-Aldrich Japan Y0001890 ネチルマイシン 硫酸塩 European Pharmacopoeia (EP) Reference Standard
European Pharmacopoeia (EP) Reference Standard
56391-57-2 Y0001890 ¥19100 2024-03-01 購入

ネチルマイシン硫酸塩 化学特性,用途語,生産方法

外観

白色~うすい黄色粉末~結晶

効能

抗生物質, タンパク質合成阻害薬

化学的特性

Off-White to Pale Beige Solid

使用

Netilmicin sulfate is used as a broad spectrum antibiotic active against most Gram-negative and some Gram-positive bacteria. It is a semisynthetic 1-N-ethyl derivative of sisomycin, an aminoglycoside antibiotic with action similar to gentamicin, but has less ear and kidney toxicity. It is used to treat gram-negative bacterial infections, gonorrhea, skin infections, and other infectious diseases. Since netilmicin sulfate cannot be absorbed from the gut, it can only be administered by injection.

主な応用

Netilmicin was synthesized by ScheringPlough Co. in 1976. The ethyl moiety was introduced at the 1-amino group of sisomicin. Its design was based on an understanding of the biochemical mechanisms of bacterial resistance to the gentamicin – sisomicin antibiotic group. The modification at the 1-amino group is known to prevent adenylation at the 2- hydroxyl group and acetylation at the 3-amino group, and to deter acetylation at the 6 -amino residue. Netilmicin shows almost the same activity against a variety of gram-positive and gram-negative bacteria as sisomicin and strong activity against gentamicin – sisomicin-resistant bacteria. It is now under study for evaluation of its clinical efficacy and safety.

臨床応用

Netilmicin sulfate, 1-N-ethylsisomicin (Netromycin), is asemisynthetic derivative prepared by reductive ethylation138of sisomicin, an aminoglycoside antibiotic obtained fromMicromonospora inyoensis. Structurally, sisomicin andnetilmicin resemble gentamicin Cla, a component of the gentamicincomplex.
Against most strains of Enterobacteriaceae, P. aeruginosa,and S. aureus, sisomicin and netilmicin are comparableto gentamicin in potency. Netilmicin is active, however,against many gentamicin-resistant strains, in particularamong E. coli, Enterobacter, Klebsiella, and Citrobacterspp. A few strains of gentamicin-resistant P. aeruginosa, S.marcescens, and indole-positive Proteus spp. are also sensitiveto netilmicin. Very few gentamicin-resistant bacterialstrains are sensitive to sisomicin, however. The potency ofnetilmicin against certain gentamicin-resistant bacteria is attributedto its resistance to inactivation by bacterial enzymesthat adenylylate or phosphorylate gentamicin and sisomicin.Evidently, the introduction of a 1-ethyl group in sisomicinmarkedly decreases the affinity of these enzymes forthe molecule in a manner similar to that observed in the1-N-ε-amino-α-hydroxybutyryl amide of kanamycin A(amikacin). Netilmicin, however, is inactivated by most of the bacterial enzymes that acetylate aminoglycosides,whereas amikacin is resistant to most of these enzymes.
The pharmacokinetic and toxicological properties ofnetilmicin and gentamicin appear to be similar clinically,though animal studies have indicated greater nephrotoxicityfor gentamicin.

ネチルマイシン硫酸塩 上流と下流の製品情報

原材料

準備製品


ネチルマイシン硫酸塩 生産企業

Global( 255)Suppliers
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ネチルマイシン硫酸塩  スペクトルデータ(MS)


56391-57-2(ネチルマイシン硫酸塩)キーワード:


  • 56391-57-2
  • D-Streptamine, O-3-deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(1→6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-α-D-glycero-hex-4-enopyranosyl-(1→4)]-2-deoxy-N1-ethyl-, sulfate (2:5)
  • Netilmicin sulfhate
  • Netilmicin sulfate(2:5)
  • Netilmicin sulphate, 1-N-Ethylsisomicin
  • 6-diamino-2,3,4,6-tetradeoxy-alpha-d-glycero-hex-4-enopyranosyl-(1-4)-6)-o-(
  • sulfate(2:5)(salt)
  • Sulfate NetilMicin
  • (2r,3r,4r,5r)-2-[(1s,2s,3r,4s,6r)-4-amino-3-[[(2s,3r)-3-amino-6-(aminomethyl)-3,4-dihydro-2h-pyran-2-yl]oxy]-6-ethylamino-2-hydroxycyclohexyl]oxy-5-methyl-4-methylaminooxane-3,5-diol sulfate (2:5)
  • Netilmicin Sulfate (500 mg)
  • O-3-Deoxy-4-C-Methyl-3-(MethylaMino)-β-l-arabinopyranosyl-(1-6)-O-[2,6-diaMino-2,3,4,6-tetradeoxy-α-D-glycero-hex-4-enopyranosyl-(1-4)]-2-deoxy-N'-ethyl-D-streptaMine
  • Netilmicin Sulfate Usp
  • Netililn
  • O-3-Deoxy-4-C-methyl-3-(methylamino)-b-l-arabinopyranosyl-(1-6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-a-D-glycero-hex-4-enopyranosyl-(1-4)]-2-deoxy-Nethyl-D-streptamine
  • D-Streptamine, O-3-deoxy-4-C-methyl-3-(methylamino)-b-L-arabinopyranosyl-(16)-O-[2,6-diamino-2,3,4,6-tetradeoxy-a-D-glycero-hex-4-enopyranosyl-(14)]-2-deoxy-N1-ethyl-, sulfate (2:5) (salt) (9CI)
  • Zetamicin
  • Netilmicin sulfate (2R,3R,4R,5R)-2-[(1S,2S,3R,4S,6R)-4-Amino-3-[[(2S,3R)-3-amino-6-(aminomethyl)-3,4-dihydro-2H-pyran-2-yl]oxy]-6-ethylamino-2-hydroxycyclohexyl]oxy-5-methyl-4-methylaminooxane-3,5-diol sulfate (2:5)
  • O-3-Deoxy-4-C-methyl-3-methylamino-ss-L-arabinopyranosyl-(1->6)-O-[2, 6-diamino-4,5-dehydro-2,3,4,6-tetradeoxy-a-D-glycero-hexopyranosyl-(1->4)]-2-deoxy-1-N-ethyl-D-streptamine hemiheptasulfate
  • O-3-Deoxy-4-C-methyl-3-(methylamino)--l-arabinopyranosyl-(1-6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-a-D-glycero-hex-4-enopyranosyl-(1-4)]-2-deoxy-N’-ethyl-D-streptamine
  • 4-O-[[3α-Amino-6-(aminomethyl)-3,4-dihydro-2H-pyran]-2α-yl]-6-O-[4-C-methyl-3-(methylamino)-3-deoxy-β-L-arabinopyranosyl]-N1-ethyl-2-deoxy-D-streptamine·2.5sulfuric acid
  • Netromycin sulfate
  • Netilmicin sulfate salt,1-N-Ethylsisomicin
  • 1-N-ETHYLSISOMICIN
  • 1-N-ETHYLSISOMICIN SULFATE
  • O-3-DEOXY-4-C-METHYL-3-METHYLAMINO-BETA-L-ARABINOPYRANOSYL-(1->6)-O-[2, 6-DIAMINO-4,5-DEHYDRO-2,3,4,6-TETRADEOXY-A-D-GLYCERO-HEXOPYRANOSYL-(1->4)]-2-DEOXY-1-N-ETHYL-D-STREPTAMINE HEMIHEPTASULFATE
  • NETILMICIN SULFATE
  • NETILMICIN SULFATE SALT
  • NETILMYCIN SULPHATE
  • NETILMICIN SULFATE USP EP
  • NETILMYCIN SULFATE USP27
  • O-3-Deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(1-6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-a-D-glycero-hex-4-enopyranosyl-(1-4)]-2-deoxy-N1-ethyl-D-streptamine sestersulfate
  • ネトロマイシン硫酸塩
  • 硫酸ネチルマイシン
  • 4-O-[[3α-アミノ-6-(アミノメチル)-3,4-ジヒドロ-2H-ピラン]-2α-イル]-6-O-[4-C-メチル-3-(メチルアミノ)-3-デオキシ-β-L-アラビノピラノシル]-N1-エチル-2-デオキシ-D-ストレプタミン·2.5硫酸塩
  • ネチルミシン硫酸塩
  • ネチルマイシン硫酸塩
  • 硫酸ネチルミシン
  • ネチルマイシン 硫酸塩
  • ネチルマイシン硫酸塩 (JAN)
  • アミノグリコシド系抗生物質
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